FDA Adverse Event Malfunction Summary report: N

HAMILTON-C3

MDR report key: 18433682 · Received January 3, 2024

Report

Report Number
3001421318-2024-00011
Event Type
Malfunction
Date Received
January 3, 2024
Date of Event
December 19, 2023
Report Date
October 18, 2024
Manufacturer
HAMILTON MEDICAL AG
Product Code
CBK
UDI-DI
07630002801881
PMA / PMN Number
K201306
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG COMES TO THE CONCLUSION: ROOT CAUSE: DEFECTIVE BUZZER (MAINBOARD). REPLACED MAINBOARD.

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG COMES TO THE CONCLUSION: ROOT CAUSE: DEFECTIVE BUZZER (MAINBOARD), REPLACED MAINBOARD. HAMILTON MEDICAL AG COMPLAINT NUMBER: (B)(4). FOLLOW-UP 1: CORRECTED INFORMATION: UDI RELATED DATA QUALITY UPDATES ONLY. FIELD D4: WAS UPDATED WITH FULL UDI INFORMATION, UPDATED FIELDS: B4, D1, D2A, D4, D8, G1, G2, G6, H2, H4, H5.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY: TF 243004 (BUZZER DEFECT AT STARTUP).

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED, TO HAMILTON MEDICAL AG: SUMMARY: TF 243004 (BUZZER DEFECT AT STARTUP).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
628333 HAMILTON-C3 HAMILTON-C3 CBK HAMILTON MEDICAL AG 160005 07630002801881

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown